FDA inspection
ResMed West Coast Warehouse: FDA inspection ending Dec 8, 2016
FDA inspection 1004382 · No Action Indicated (NAI) · Moreno Valley, CA
Key facts
| Inspection ID | 1004382 |
|---|---|
| Firm | ResMed West Coast Warehouse |
| FEI number | 3007009701 |
| Address | 23650 Brodiaea Ave |
| City | Moreno Valley |
| State | CA |
| ZIP | 92553-8816 |
| Fiscal year | 2017 |
| Inspection end date | Dec 8, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data